| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128881925-128882182 | Common:1; Rare:86 | ||||
| chr9:128947543-128947725 | Common:1; Rare:83; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129110667-129110950 | Common:3; Rare:63 | ||||
| chr9:129803053-129803175 | Common:2; Rare:36 | ||||
| chr9:129835225-129835475 | Common:2; Rare:99 | ||||
| chr9:130053816-130053929 | Common:1; Rare:38 | ||||
| chr9:131502892-131503044 | Rare:54; Clinvar:3 | ||||
| chr9:132354926-132355186 | Common:3; Rare:85 | ||||
| chr9:132878269-132878414 | Common:1; Rare:57 | ||||
| chr9:133030471-133030792 | Common:4; Rare:89 | ||||
| chr9:133163910-133164012 | Common:3; Rare:25 | ||||
| chr9:133348039-133348237 | Common:2; Rare:72 | ||||
| chr9:133356425-133356601 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375936-133376413 | Common:5; Rare:166 | ||||
| chr9:133417953-133418110 | Common:2; Rare:39 |